HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → HCID 11219535, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 22939251 | HCID 22939251 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11219535 | HCID 11219535 | 100% |
Reaction Steps
Into a solution of 2.30 g (6.33 mmol) of 4-isopropyl-3-(1-benzylpiperidin-4-yl)-3,4-dihydro-2(1H)-quinazolinone in 127 ml of methanol, 0.23 g (0.11 mmol) of 10% palladium carbon (50% wet) and 1.60 g (25.3 mmol) of ammonium formate were added and refluxed under stirring and heating for 4 hours. After cooling to room temperature, the reaction mixture was filtered. To the filtrate, 0.5% aqueous sodium hydroxide solution and chloroform were added and stirred. The separated oil layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The concentrated residue was purified by silica gel column chromatography (chloroform/methanol/triethylamine 90/10/5) to give 1.73 g (6.33 mmol) of the above-titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07329665B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-fd78dfee215447b4ba54d0210624c204 |
| Source note | uspto-grants-2008_02 |